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Profile Name | CD274 over exp |
Gene Variant Detail | |
Relevant Treatment Approaches | PD-L1/PD-1 antibody |
Molecular Profile | Indication/Tumor Type | Response Type | Therapy Name | Approval Status | Evidence Type | Efficacy Evidence | References |
---|---|---|---|---|---|---|---|
CD274 over exp STK11 mut | lung adenocarcinoma | not predictive | unspecified immune checkpoint inhibitor | Clinical Study - Cohort | Actionable | In a clinical study, lung adenocarcinoma patients with high expression of CD274 (PD-L1; >/= 50%) and a co-occurring STK11 mutation demonstrated a similar objective response rate (P=0.2), progression-free survival (P=0.29), and overall survival (0.44) compared to patients with negative expression of CD274 (PD-L1) and a co-occurring EGFR mutation when treated with an unspecified immune checkpoint inhibitor (PMID: 32178965). | 32178965 |
CD274 over exp TP53 mut | lung adenocarcinoma | predicted - sensitive | unspecified immune checkpoint inhibitor | Clinical Study - Cohort | Actionable | In a clinical study, lung adenocarcinoma patients with high expression of CD274 (PD-L1; >/= 50%) and a co-occurring TP53 mutation demonstrated a greater objective response rate, 39.8% (35/88) vs 18.3% (13/71); P=0.005, progression-free survival (HR=0.62, P=0.006), and overall survival (HR=0.65, P=0.04) compared to patients with negative expression of CD274 (PD-L1) and a co-occurring KRAS mutation when treated with an unspecified immune checkpoint inhibitor (PMID: 32178965). | 32178965 |
ALK rearrange CD274 over exp | lung adenocarcinoma | predicted - sensitive | Atezolizumab + Bevacizumab + Carboplatin + Pemetrexed Disodium | Case Reports/Case Series | Actionable | In a clinical case study, a patient with ALK-rearranged lung adenocarcinoma with high CD274 (PD-L1) expression (TPS>=50%) who progressed on 3 prior ALK inhibitors experienced a rapid and ongoing clinical improvement with the combination therapy of Tecentriq (atezolizumab), Avastin (bevacizumab), Paraplatin (carboplatin), and Alimta (Pemetrexed Disodium), achieving decreased lung lesion size, complete metabolic response of liver lesions, and partial response of bone lesions (PMID: 34336591). | 34336591 |
CD274 over exp POLE R34L | small intestine adenocarcinoma | predicted - sensitive | Pembrolizumab | Case Reports/Case Series | Actionable | In a clinical case study, Keytruda (pembrolizumab) treatment resulted in a reduction of primary tumor and metastatic lesions and an ongoing progression-free survival at 31 months in a patient with microsatellite stable (MSS) ileum adenocarcinoma that had high CD274 (PD-L1) expression (TPS = 75%) and harbored POLE R34L, but had low tumor mutational burden (PMID: 34875656). | 34875656 |
CD274 over exp STK11 A205Rfs*82 | lung squamous cell carcinoma | predicted - resistant | Pembrolizumab | Case Reports/Case Series | Actionable | In a clinical case study, a lung squamous cell carcinoma patient with high CD274 (PD-L1) expression progressed after initial response to Keytruda (pembrolizumab) and through subsequent ctDNA testing was found to have acquired STK11 A205Rfs*82 (PMID: 33832284). | 33832284 |
BRAF V600E CD274 over exp | lung adenocarcinoma | predicted - sensitive | Dabrafenib + Trametinib | Case Reports/Case Series | Actionable | In a clinical case study, second-line treatment with the combination of Tafinlar (dabrafenib) and Mekinist (trametinib) resulted in a clinical response lasting at least 5 years in a patient with lung adenocarcinoma harboring BRAF V600E and high CD274 (PD-L1) expression (TPS=100%) who did not respond to first-line Keytruda (pembrolizumab) (PMID: 38429896). | 38429896 |